4.8 Article

A wavelength-induced frequency filtering method for fluorescent nanosensors in vivo

Journal

NATURE NANOTECHNOLOGY
Volume 17, Issue 6, Pages 643-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41565-022-01136-x

Keywords

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Funding

  1. Koch Institute for Integrative Cancer Research at MIT
  2. Bridge Project Program
  3. Swiss National Science Foundation [P2ELP3_162149, P300P2_174469]
  4. Japan Society for the Promotion of Science [15J07423, JP16K17485]
  5. King Abdullah University of Science Technology [OSR-2015 Sensors 2707]
  6. Zuckerman STEM Leadership Program
  7. Israeli Science Foundation [456/18]
  8. Arnold O. Beckman Postdoctoral Fellowship from the Arnold and Mabel Beckman Foundation
  9. Grants-in-Aid for Scientific Research [15J07423] Funding Source: KAKEN
  10. Swiss National Science Foundation (SNF) [P2ELP3_162149, P300P2_174469] Funding Source: Swiss National Science Foundation (SNF)

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This research introduces a new technique (WIFF) to overcome the limitations of fluorescent nanosensors in vivo. By modulating the excitation wavelength, WIFF improves the signal-to-noise ratio and enables tracking and monitoring of various substances' responses in deep tissues, including drug metabolites. This capability is significant for life sciences research, therapeutics, and medical diagnostics.
Fluorescent nanosensors hold the potential to revolutionize life sciences and medicine. However, their adaptation and translation into the in vivo environment is fundamentally hampered by unfavourable tissue scattering and intrinsic autofluorescence. Here we develop wavelength-induced frequency filtering (WIFF) whereby the fluorescence excitation wavelength is modulated across the absorption peak of a nanosensor, allowing the emission signal to be separated from the autofluorescence background, increasing the desired signal relative to noise, and internally referencing it to protect against artefacts. Using highly scattering phantom tissues, an SKH1-E mouse model and other complex tissue types, we show that WIFF improves the nanosensor signal-to-noise ratio across the visible and near-infrared spectra up to 52-fold. This improvement enables the ability to track fluorescent carbon nanotube sensor responses to riboflavin, ascorbic acid, hydrogen peroxide and a chemotherapeutic drug metabolite for depths up to 5.5 +/- 0.1 cm when excited at 730 nm and emitting between 1,100 and 1,300 nm, even allowing the monitoring of riboflavin diffusion in thick tissue. As an application, nanosensors aided by WIFF detect the chemotherapeutic activity of temozolomide transcranially at 2.4 +/- 0.1 cm through the porcine brain without the use of fibre optic or cranial window insertion. The ability of nanosensors to monitor previously inaccessible in vivo environments will be important for life-sciences research, therapeutics and medical diagnostics. An optical technique is developed that extends the capabilities of fluorescent nanosensors into previously inaccessible ultradeep in vivo locations, including the brain, without the use of fibre optic or cranial window insertion.

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